Molecular insights into the premature aging disease progeria

Hutchinson–Gilford progeria syndrome (HGPS) is an extremely rare premature aging disease presenting many features resembling the normal aging process. HGPS patients die before the age of 20 years due to cardiovascular problems and heart failure. HGPS is linked to mutations in the LMNA gene encoding...

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Detalles Bibliográficos
Autores principales: Vidak, Sandra, Foisner, Roland
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4796323/
https://www.ncbi.nlm.nih.gov/pubmed/26847180
http://dx.doi.org/10.1007/s00418-016-1411-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4796323/
https://www.ncbi.nlm.nih.gov/pubmed/26847180
http://dx.doi.org/10.1007/s00418-016-1411-1

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